Optical material and process for making the same

ABSTRACT

An optically transmittant body comprising a solid solution of a ternary sulfide and a selected binary sulfide such as a solid solution of calcium lanthanum sulfide and phase lanthanum sulfide is provided by precipitating out of a nitrate solution of calcium and lanthanum, a starting powder of calcium carbonate and lanthanum carbonate. The molar ratio of lanthanum to calcium is greater than 2.0 moles lanthanum to 1.0 moles of calcium nitrate. The starting powder is reacted with a sulfurizing agent such as hydrogen sulfide to convert such starting powder into a powder of the solid solution of calcium lanthanum sulfide and phase lanthanum sulfide. The precipitate ion reaction forms a homogenous fine particle size starting powder of calcium carbonate and lanthanum carbonate which is substantially and uniformly converted into the solid solution powder. The phase lanthanum sulfide has a similar crystallographic structure as the calcium lanthanum sulfide. The solid solution of calcium lanthanum sulifide and the phase lanthanum sulfide powder is then compacted into the desired form of the optically transmittant body, and is then sintered at an elevated temperature in an atmosphere of excess sulfur to increase the density of the compacted body. An atmosphere including sulfur is provided to prevent decomposition of the material and to aid in the conversion of any residual, unsulfurized calcium carbonate, lanthanum carbonate materials present in the solid solution. The sintered material is then compressed at an elevated pressure and temperature providing the material of the optically transmittant body.

This application is a continuation of application Ser. No. 500,703 filed 6-03-83, now abandoned.

BACKGROUND OF THE INVENTION

This invention relates generally to optical materials and more particularly to materials which have improved optical transmittance for far infrared electromagnetic radiation.

As is known in the art, optically transmittant materials are used in fabricating optical windows for use in various optical detection applications. In particular, such materials are used as domes and windows in heat seeking missile applications. When used in such applications, the selected material for a given thickness must be sufficiently transmittant to infrared electromagnetic radiation to enable sensitive detection of such radiation, and must be sufficiently durable to withstand mechanical forces encountered during the missile's flight. Further, the selected material must also be resistant to rain erosion, damage caused by high velocity water droplets impinging on the material during flight.

One material which has been suggested for such application is calcium lanthanum sulfide (CaLa₂ S₄). Calcium lanthanum sulfide is one of a class of materials known as ternary sulfides. These materials are characterized by having two cations in chemical combination with a sulfide S² - ion as the anion of the compound. One method used in the prior art for fabricating such ternary sulfide material as described in an article, by Pennsylvania State University, entitled "Ternary Sulfide Infrared Window Materials," First Annual Report to the Office of Naval Research, Contract Number N00014-80-C-0526 (May 1, 1980-Oct. 31, 1981), AD-A120 153/2 Index 4 February 1983, includes the step of spray drying calcium and lanthanum ions from a solution of calcium nitrate and lanthanum nitrate in an atmosphere of oxygen to form a starting powder of calcium oxide powder and lanthanum oxide powder. The starting powder is then sulfurized to provide calcium lanthanum sulfide powder. The resulting powder is further processed to form a compact, densified body of calcium lanthanum sulfide material. While the spray drying of calcium and lanthanum ions is an adequate process for producing calcium lanthanum sulfide material, such a process may be costly, and further, the degree of optical transmittance provided by such material is less than the theoretical maximum transmittance. A second method known in the art to produce a calcium lanthanum sulfide compound is a technique commonly referred to as solid state reaction processing. This involves producing a starting powder by mixing powders of calcium carbonate and lanthanum oxide, and sulfurizing the starting powder to produce the calcium lanthanum sulfide material. While this latter method is less costly and simpler compared with the former method, material produced by the latter method has reduced transmittance. More particularly, with the latter method an x-ray diffraction pattern of the produced calcium lanthanum sulfide material indicates the presence of the binary sulfide, calcium sulfide. Since calcium sulfide has a substantially different crystallographic structure than calcium lanthanum sulfide, the presence of calcium sulfide is believed to cause the reduced transmittance of calcium lanthanum sulfide material produced with the latter method. Further, solid state reaction processing of commercially available calcium carbonate and lanthanum oxide powders provides a starting powder having a very large variation in powder particle size. Due to the presence of very large agglomerated particles of lanthanum oxide, the sulfurization process is very slow, necessitating the use of a particle size reduction process such as jet milling prior to sulfurization. Jet milling, or similar techniques of particle size reduction, reduces some of the cost advantages of the latter method over the former method and also introduces impurities into the powder which are believed to degrade optical properties of the resulting calcium lanthanum sulfide.

With calcium lanthanum sulfide powder formed by either of the above methods, the powder is then molded into a compact body and then the body is densified to provide the compact, densified body. Several different densifying steps are generally performed in order to densify the material. In general, however, powders fabricated by either method described above generally require the step of conventional hot pressing in the densification process to provide bodies with high density. Hot pressing involves compression of the compact body in a single or uniaxial direction at an elevated temperature. While hot pressing is a conventional processing technique, its elimination is highly desirable because, in general, hot pressing can be performed only on a single body at a time thus increasing product cost.

SUMMARY OF THE INVENTION

In accordance with the present invention, a binary sulfide produced during production of a ternary sulfide has substantially the same crystallographic structure as that of the ternary sulfide to provide, after densification, an optical material having an improved optical transmittance. The binary sulfide and the ternary sulfide are formed by: (1) selecting both a pair of cations of the ternary sulfide and the composition ratio of the pair of cations of the ternary sulfide to provide a predetermined excess amount of a selected one of said pair of cations in relation to the remaining one of said pair of cations; and, (2) subsequently converting the pair of cations into the ternary sulfide by reacting the pair of cations with sulfur, and the excess amount of the selected one of the pair of cations being converted into the binary sulfide. With such method, optically transmittant bodies fabricated therefrom have improved optical transmittance properties because the selected binary sulfide, having substantially the same crystallographic structure as the ternary sulfide, will be in solid solution with the ternary sulfide. Thus, by forming the binary sulfide with the same crystallographic structure as the ternary sulfide, the detrimental effect on optical properties generally associated with mixtures of binary sulfides and ternary sulfides having different crystallographic properties is eliminated.

In accordance with an additional aspect of the present invention, a transmittant body of a solid solution of calcium lanthanum sulfide and γ phase lanthanum sulfide is provided by selecting a composition ratio of calcium and lanthanum to provide a starting material having an excess amount of lanthanum to calcium in a ratio of greater than 2.0 moles of lanthanum to 1.0 mole of calcium, and processing said starting powder to form the solid solution of calcium lanthanum sulfide and γ phase lanthanum sulfide material. With such starting powder, formation of a solid solution including γ phase lanthanum sulfide is seen to provide two advantages which enhance optical properties of resulting bodies made with such method. Firstly, providing excess lanthanum combines any uncombined calcium therewith to form additional calcium lanthanum sulfide and thus eliminates formation of the undesirable binary sulfide, calcium sulfide whose presence in calcium lanthanum sulfide material is generally detrimental to optical transmittant properties of calcium lanthanum sulfide material. Secondly, the γ phase lanthanum sulfide has a crystallographic structure which is substantially similar to calcium lanthanum sulfide forming a solid solution with calcium lanthanum sulfide, and resulting in material having substantially improved optical transmittance properties. Additionally, by forming γ phase lanthanum sulfide, the composition ratio of calcium to lanthanum is less critical in that the critical amount of lanthanum is selected only in relation to the amount of calcium provided, with any excess amount of lanthanum being processed to form the desirable γ phase lanthanum sulfide.

BRIEF DESCRIPTION OF THE DRAWINGS

The aforementioned aspects and other features of the invention are explained in the following description taken in connection with the accompanying drawings, in which:

FIG. 1 is a process flow diagram showing steps in the method of fabricating a ternary sulfide calcium lanthanum sulfide, optical material;

FIG. 2A is a scanning electron microscope (SEM) photomicrograph at a magnification of 200X of intermixed calcium carbonate and lanthanum oxide powders provided in accordance with a prior art technique detailing particle size of such powders;

FIG. 2B is an SEM photomicrograph at a magnification of 200X of co-precipitated homogenously mixed calcium carbonate and lanthanum carbonate powders provided in accordance with FIG. 1 showing detailed particle size of such powders;

FIG. 3A is a photomicrograph from an optical microscope at a magnification of 187X of a portion of a body of the calcium lanthanum sulfide material fabricated in accordance with FIG. 1 detailing microstructure of the body after sintering;

FIG. 3B is a photomicrograph from an optical microscope at a magnification of 187X of a portion of the body of calcium lanthanum sulfide shown in FIG. 3A fabricated in accordance with FIG. 1 detailing microstructure of the body after hot isostatic pressing;

FIG. 4A is a graph of X-ray intensity versus diffraction angle (2θ) for an x-ray diffraction analysis of a typical sample of calcium lanthanum sulfide material fabricated in accordance with the prior art technique of FIG. 2A;

FIG. 4B is a graph of X-ray intensity versus diffraction angle (2θ) for an x-ray diffraction analysis of a sample of calcium lanthanum sulfide material fabricated in accordance with FIG. 1 after sulfurization;

FIG. 5 is a graph of percent transmittance versus wavelength of two samples having different thicknesses of the calcium lanthanum sulfide material of FIG. 4B;

FIG. 6 is a process flow diagram showing steps in the method of fabricating a ternary sulfide and binary sulfide solid solution, such as, a solid solution of calcium lanthanum sulfide and phase lanthanum sulfide;

FIG. 7 is an SEM photomicrograph at a magnification of 5000X of calcium lanthanum sulfide and lanthanum sulfide powder/fabricated in accordance with FIG. 6;

FIG. 8A is a photomicrograph from a optical microscope at a magnification of 187X of a portion of a body of the calcium lanthanum sulfide and phase lanthanum sulfide material fabricated in accordance with FIG. 6 detailing the microstructure of the body after sintering;

FIG. 8B is a photomicrograph from an optical microscope at a magnification of 187X of a portion of the body of FIG. 4A detailing the microstructure of the body after hot isostatic pressing;

FIG. 9 is a graph of X-ray intensity versus diffraction angle for an x-ray diffraction analysis of the solid solution material of FIG. 7; and

FIG. 10 is a graph of percent transmittance versus wavelength of two samples having different thicknesses of the material of FIG. 8B.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

A process for fabricating an optically transmittant body will initially be described in conjunction with the process flow diagram of FIG. 1.

Referring now to FIG. 1, an ionic solution of here metal cations and nitrate anions is prepared to provide a source of such metal cations. The metal cations selected are calcium and lanthanum although other cations such as strontium and neodymium or a single cation such as lanthanum may be used. Here, 12.5 grams of hydrous, crystalline calcium nitrate (Ca(NO₃)₂.4H₂ O and 47.3 grams of hydrous, crystalline lanthanum nitrate (La(NO₃)₃. 6H₂ O) are dissolved in 175 ml of distilled water (H₂ O) to form an ionic solution wherein the calcium cations and lanthanum cations disassociate from the nitrate anions. (A hydrous crystal is a crystal within which water molecules are combined with molecules of the crystal). The above-mentioned hydrate characteristics of the calcium nitrate (.4H₂ O) and the lanthanum nitrate (.6H₂ O) are approximate characteristics and such materials are distributed by VWR Scientific Inc., Boston, Mass., Catalog No.'s 1395-5 and P354, respectively. Calcium nitrate and lanthanum nitrate sources of calcium and lanthanum ions (Ca⁺², La ⁺³) are selected because of their relatively high solubility in water. The above-described ionic solution provides an adequate source of calcium and lanthanum cations used to fabricate optically transmittant ternary calcium lanthanum sulfide material in a manner to be described. The cation solution of calcium and lanthanum is prepared by first dissolving the crystals of calcium nitrate and the crystals of lanthanum nitrate in water at a temperature of approximately 22° C. The temperature of the ionic solution is then gradually raised to approximately 40° C. During this interval, the solution of calcium and lanthanum nitrates is constantly stirred to intermix the calcium ions, lanthanum ions and nitrate ions in solution.

A precipitating agent solution is here prepared by mixing 47.1 grams of ammonium carbonate with 125 ml of water. The ammonium carbonate is believed to be an anhydrous crystal, that is, a crystal without water molecules combined with the crystal molecules. The ammonium carbonate here is distributed by Thiokol/Ventron Division, Andover Street, Danvers, Mass., Catalog No. 303352. The precipitating solution is prepared by adding the ammonium carbonate to the water which is at a temperature of approximately 22° C. The temperature of the ammonium carbonate solution is then gradually elevated to a temperature of approximately 40° C., while the ammonium carbonate is constantly stirred to provide a source of ammonium ions and carbonate ions in the precipitating agent solution. The ammonium carbonate precipitating agent solution is then gradually added to the calcium lanthanum nitrate ionic solution. As the ammonium carbonate solution is added to the constantly stirred ionic solution of calcium and lanthanum nitrates, two ionic reactions take place wherein calcium carbonate precipitate and lanthanum carbonate precipitate are concurrently formed as precipitate reaction products in accordance with ionic reactions 1 and 2:

    Ca.sup.-2 +C.O.sub.3.sup.+2 →CaCO.sub.3             (Reaction 1)

    2La.sup.-3 +3CO.sub.3.sup.+2 →La.sub.2 (CO.sub.3).sub.3 (Reaction 2)

After complete addition of the ammonium carbonate solution, the nitrate solution and the precipitates are mixed in the mixing vat for approximately ten minutes to insure complete precipitation of calcium carbonate and lanthanum carbonate from the nitrate solution and to provide a homogeneous mixture of calcium carbonate precipitate and lanthanum carbonate precipitate. The intimately mixed precipitates, (i.e. the co-precipitate) of calcium carbonate and lanthanum carbonate, facilitate conversion of such calcium and lanthanum sources into the calcium lanthanum sulfide material during subsequent sulfurization in a manner to be described.

The co-precipitate of calcium carbonate and lanthanum carbonate is then filtered from the nitrate solution, cleaned by using distilled water, and is then dried in a vacuum oven at approximately 110° C. for twenty-four to seventy-two hours. A highly agglomerated homogeneous, intimately mixed mass of calcium carbonate and lanthanum carbonate is provided after drying of the precipitate. It is to be noted, however, that the calcium carbonate and lanthanum carbonate are believed to be in hydrous form, having a heretofore undetermined amount of water molecules which are in combination with the calcium carbonate and lanthanum carbonate molecules.

As previously mentioned, the calcium carbonate and the lanthanum carbonate are intimately mixed and uniformly distributed throughout the agglomerated mass. The calcium carbonate and lanthanum carbonate agglomerated mass is broken up into a starting powder, as shown in FIG. 2B, by conventional techniques such as using a mortar and pestle prior to further processing of such material.

As shown in FIG. 2A, a scanning electron microscope (SEM) photomicrograph reveals the detailed microstructure of a mixture of calcium carbonate and lanthanum oxide powder processed by conventional solid state reaction. The small cubic-like structures are believed to be calcium carbonate particles whereas the lanthanum oxide particles are believed to be particles which range in size from the dust-size particles to the large agglomerated chunks. Thus, as previously described, a large variation in size between calcium carbonate and lanthanum oxide powders as well as a large variation in size between the lanthanum oxide particles in general, as understood, hinders formation of the calcium lanthanum sulfide powder. To improve such formation, intermediate steps such as jet milling of the powder to reduce the particle size of the agglomerated lanthanum oxide powders in particular is generally required. As previously mentioned, such a step generally, as understood, introduces unwanted impurities into the powders.

Concurrently forming precipitates of calcium carbonate and lanthanum carbonate provides a fine-grained, homogeneously mixed starting powder which is more readily converted into the calcium lanthanum sulfide during subsequent sulfurization. As shown in FIG. 2B, a SEM photomicrograph of the calcium carbonate and lanthanum carbonate starting powder reveals a microstructure having particles which are substantially uniform and small in size. Absent are the large agglomerated particles of lanthanum carbonate, as shown in FIG. 2A. Thus, due to the intimately, homogeneously mixed starting powder and the reduced particle size of the calcium carbonate and lanthanum carbonate starting powder, formation of the calcium lanthanum sulfide powder is more readily accomplished during sulfurization, in a manner to be described, without the need for intermediate processing steps such as jet milling.

The starting powder is then sulfurized to convert such starting powder into the calcium lanthanum sulfide. This is accomplished as follows. The intimately mixed calcium carbonate and lanthanum carbonate starting powder is disposed in an alumina boat, and the alumina boat is then placed in an alumina reaction tube furnace. The interior of the tube is purged of atmospheric gases by directing a continuous flow of helium or another inert gas into the tube. The flow rate for the helium gas is typically 20 SCCM (standard cubic centimeters per minute). The furnace is then raised to a predetermined, elevated temperature, typically in the range of 900° C. to 1100° C. A preferred elevated temperature of 1000° C. is here used. At the preferred elevated temperature of 1000° C. and with the continuous flow of helium gas, a predetermined continuous flow rate of hydrogen sulfide gas (H₂ S) is directed over the calcium carbonate and lanthanum carbonate starting powder. Here the flow rate for the hydrogen sulfide gas for 35.1 grams of calcium carbonate and lanthanum carbonate starting powder is 80 SCCM. A continuous flow of hydrogen sulfide is provided for here approximately 20 hours at 1000° C. In response to such flow of hydrogen sulfide at the elevated temperature, a reaction takes place by diffusion of sulfur into the carbonate powder in accordance with reaction 3 to provide the calcium lanthanum sulfide:

    La.sub.2 (CO.sub.3).sub.3 +CaCO.sub.3 +4H.sub.2 S→CaLa.sub.2 S.sub.4 +4H.sub.2 O+4CO.sub.2                                     (Reaction 3)

The calcium lanthanum sulfide material is also a well-agglomerated mass which is broken up into smaller sized particles to increase the surface area of the material. The technique here used to break up the material is to grind the material with a mortar and pestle with a predetermined amount of methanol having previously been added to the material. The material and the methanol are intermixed for one to two minutes. A 400 mesh sieve is then used to filter out particles having a dimension greater than 37 microns. The filtered calcium lanthanum sulfide material is then dried out by evaporating the methanol to provide a powder of calcium lanthanum sulfide.

Having formed the calcium lanthanum sulfide powder, the powder is then processed into the optically transmittant body. The processing for shaping the body is here as follows: The powder is first molded into the shape of body by placing the powder in a mold and pressing the powder into the desired shape. The molded powder is further processed by cold isostatically pressing the molded powder to consolidate the powder and provide calcium lanthanum sulfide material with an actual density of approximately 60% of the theoretical density of such material. As is known in the art, cold isostatic pressing involves isostatic compression of material by a fluid introduced into a vessel at an elevated pressure and constant temperature. A fluid, typically a liquid, surrounds the material previously sealed under a vacuum in a rubber enclosure, and exerts a pressure of here 25,000 psi substantially uniformly in all directions on the material to consolidate the material. After consolidation of the material, the material is sintered.

During sintering, the calcium lanthanum sulfide material is placed on a setter plate, here comprised of boron nitride. The setter plate is then disposed in a graphite resistance furnace. The internal atmosphere of the graphite resistance furnace is then placed under a vacuum and backfilled with an inert gas such as helium to remove atmospheric gases. The temperature of such furnace is elevated to a temperature in the range of 1000° C. to 1400° C. with 1150° C. being the preferred temperature, while maintaining atmospheric pressure and a continuous helium flow in the furnace. Sintering takes place at the elevated temperature of 1150° C. for approximately sixteen hours by passing the continuous flow of helium having a flow rate of here 50 SCCM and a reactive gas, here hydrogen sulfide, having a flow rate of here 15 SCCM across the material disposed on the boron nitride plate. The presence of the hydrogen sulfide gas during sintering aids in preventing decomposition of the calcium lanthanum sulfide material at the elevated temperature by preventing sulfur from leaving the calcium lanthanum sulfide material. The sulfur rich environment might also aid in the conversion of any unconverted calcium carbonate or lanthanum carbonate material or any material deficient in sulfur which still might be present in the consolidated material. After sintering, the calcium lanthanum sulfide material has an actual density in the range of approximately 91 to 95% of its theoretical density.

As shown in FIG. 3A, the microstructure of the surface of the body is comprised of isolated closed pores and small grains of such material.

The material after sintering is wrapped in a platinum foil and is then processed by a technique commonly referred to as hot isostatic pressing. Hot isostatic pressing involves the compression of a material at an elevated temperature and pressure in a nonreactive gas environment such as nitrogen or one of the noble gases, such as argon. Argon is here introduced into the vessel at room temperature (22° C.) to an elevated pressure of approximately 8000 psi. The temperature of the vessel is then elevated to a temperature in the range of 900° C. to 1100° C., here 990° C. raising the pressure of the argon in response thereto to a pressure in the range of 25,000 psi to 29,000 psi. Such pressure is exerted on the body substantially uniformly in all directions. The body is maintained at these conditions for approximately three hours. At the completion of this process, a body having a density of at least 99.5% of the theoretical density of such material is obtained.

As shown in FIG. 3B, the microstructure of the surface of the body after hot isostatic pressing provides material having substantially no porosity without changing the grain size of the material provided during the sintering step. The fabricated body is then ground and polished to predetermined specifications of thickness and surface quality using conventional techniques.

With the above-described process, several advantages in providing bodies comprising ternary sulfides is provided.

Again, as shown in FIG. 2A, a (SEM) photomicrograph reveals the detailed microstructure of a calcium carbonate (small cubes) and lanthanum oxide (large agglomerated particles and background particles) mixture for solid state reaction conversion to calcium lanthanum sulfide. As previously described in the Background of the Invention section, this technique involves the steps of mixing pure calcium carbonate and pure lanthanum oxide particles such as that shown in FIG. 2A and then sulfurizing the mixture to provide calcium lanthanum sulfide. It is to be noted that calcium carbonate is in the form of relatively small cubes whereas the lanthanum oxide particles vary in size from very fine powder to the very large agglomerated masses. Thus, with this approach, there is believed to be an unequal reaction rate of the prepared powders with sulfur, and as a result, complete conversion of calcium and lanthanum to calcium lanthanum sulfide is hindered. Further, material made with this method generally includes the binary sulfide calcium sulfide. The presence of calcium sulfide in the calcium lanthanum sulfide is believed responsible in part, for degraded optical properties of the calcium lanthanum sulfide material manufactured in accordance with such method and in other prior art techniques.

As shown in FIG. 4A, an x-ray diffraction pattern of a calcium lanthanum sulfide material made from the conventional solid state reaction of calcium carbonate and lanthanum oxide such as that described above in conjunction with FIG. 2A by passing hydrogen sulfide gas over the sample for 100 hours at 1060° C. depicts peaks 40 and 42 which occur at a diffraction angles of 20θ=31.5° and 2θ=45° indicating the presence of calcium sulfide. The presence of calcium sulfide in the calcium lanthanum sulfide is undesirable, as understood, because of the crystallographic dissimilarities of calcium sulfide to the calcium lanthanum sulfide. The presence of calcium sulfide is believed to provide a reduction in the desired optical transmittance properties of the calcium lanthanum sulfide material. Thus, the presence of the calcium sulfide in calcium lanthanum sulfide material is highly undesirable.

Again, as shown in FIG. 2B, an SEM photomicrograph shows the mixed calcium carbonate and lanthanum carbonate starting powder provided as a result of concurrently precipitating calcium carbonate and lanthanum carbonate from the nitrate solution in accordance as described above. As shown, the co-precipitated calcium carbonate and lanthanum carbonate particles are intimately mixed, providing a homogenous starting powder, and are of relatively small and substantially uniform particle size. Sulfurization of such starting powder to provide the calcium lanthanum sulfide is significantly easier and provides substantially complete conversion of the calcium carbonate and lanthanum carbonate to the calcium lanthanum sulfide. Further, since the particle sizes are relatively small thereby having increased particle surface area, the amount of time required for such conversion is substantially decreased from the above-mentioned solid state reaction method.

Referring now to FIG. 4B, an x-ray diffraction pattern of a sample of calcium lanthanum sulfide material made from the co-precipitation (i.e. concurrent precipitation) of calcium carbonate and lanthanum carbonate and sulfurized for twenty hours in a helium/hydrogen sulfide atmosphere at an elevated temperature of 1000° C. is shown. It is noted that the peaks 40, 42 (FIG. 5A) generally associated with the calcium sulfide, as depicted in FIG. 4A, are substantially eliminated from the X-ray diffraction analysis of FIG. 4B. Thus, it is believed that the calcium sulfide has been substantially reduced. However, as can be seen in FIG. 4B, at 2θ=45° there appears to be a very small peak 41 present indicating that there still may be a small amount of calcium sulfide contained in the calcium lanthanum sulfide. Thus, the calcium lanthanum sulfide material fabricated from the co-precipitation of calcium carbonate and lanthanum carbonate is substantially absent of calcium sulfide and thus is believed to be a substantially phase-pure composition.

Referring now to FIG. 5, a graph of in-line infrared percent transmittance for the calcium lanthanum sulfide material fabricated in accordance with FIG. 1 is shown for a sample (a) having a thickness of 0.011 inches (curve a) and a sample (b) having a thickness of 0.049 inches (curve b).

                  TABLE 1                                                          ______________________________________                                                  % Transmittance T.sub.a                                                                      % Transmittance T.sub.b                                 Wavelength                                                                              Sample A      Sample B      α                                   (micron) t.sub.a = 0.011 inches                                                                       t.sub.b = 0.049 inches                                                                       (cm.sup.-1)                               ______________________________________                                          4       50            17            11                                         6       51            18            11                                         8       52            20            10                                        10       54            21            10                                        12       56            23             9                                        14       56            23             9                                        16       56            21            10                                        18       46             6            52                                        ______________________________________                                    

From the values of percent transmittance from each curve a, b, a characteristic of the material which indicates the absorption of the material for electromagnetic radiation in the range of 4 microns to 18 microns is obtained from the equation α=|-ln (T_(b) /T_(a))|(t_(b) -t_(a)), where α is a quantity referred to as the "coefficient of absorption," T_(a), T_(b) are the percent transmittance of samples a, b, respectively, and t_(a), t_(b) are the thicknesses of samples a, b. For material fabricated in accordance with FIG. 1, α is in the range of 9 cm⁻¹ to 11 cm⁻¹ to electromagnetic radiation having a wavelength in the range of 4 microns to 16 microns.

Referring now to FIG. 6, a process is described for fabricating an optically transmittant body of ternary sulfide having an in-line percent transmittance greater than that produced by the process described in connection with FIG. 1. Here again an ionic solution of metal cations and nitrate anions is prepared to provide a source of such metal cations. The metal cations selected are calcium and lanthanum although other cations such as strontium and neodymium may be used. Here, 22.1 grams of hydrous, crystalline calcium nitrate (Ca(NO₃)₂.4H₂ O) and 108.3 grams of hydrous, crystalline lanthanum nitrate (La(NO₃)₃.6H₂ O) are dissolved into 300 ml of distilled water (H₂ O) to form an ionic solution wherein the calcium and lanthanum cations disassociate from the nitrate anions. The above-mentioned hydrate characteristics of the calcium nitrate (.4H₂ O) and the lanthanum nitrate (.6H₂ O) are approximate characteristics and such materials are distributed by VWR Scientific Inc., Boston, Mass., as previously mentioned. Calcium nitrate and lanthanum nitrate sources of calcium and lanthanum ions (Ca⁺², La⁺³) are again selected because of their relatively high solubility in water. The above-described ionic solution was chosen to provide an excess amount of lanthanum ions in relation to calcium ions. A ratio of at least 4.1 grams of lanthanum nitrate to 1 gram of calcium nitrate is used, with a ratio of approximately 5 grams of lanthanum nitrate to 1 gram of calcium nitrate here being the preferred ratio. Alternatively, more than 2.0 moles of lanthanum per 1.0 moles of calcium is used to provide the excess lanthanum in the solution. The cation solution of calcium and lanthanum is prepared by first dissolving the crystals of calcium nitrate and the crystals of lanthanum nitrate in water at a temperature of approximately 22° C. The temperature of the solution is then gradually raised to approximately 40° C. During this interval, the solution of calcium and lanthanum nitrates is constantly stirred to intermix the calcium ions, lanthanum ions and nitrate ions in solution.

A precipitating agent solution is here prepared by mixing 81.2 grams of ammonium carbonate with 214 ml of water. The ammonium carbonate here used is distributed by Thiokol/Ventron Division, Danvers, Mass., as previously described. The precipitating solution is prepared by adding the ammonium carbonate to the water which is at a temperature of approximately 22° C. The temperature of the ammonium carbonate solution is then gradually elevated to a temperature of approximately 40° C., while the ammonium carbonate is constantly stirred to provide a source of ammonium ions and carbonate ions in the precipitating agent solution. The ammonium carbonate precipitating agent solution is then gradually added to the calcium lanthanum nitrate ionic solution. As the ammonium carbonate solution is added to the constantly stirred ionic solution of calcium and lanthanum nitrates, two ionic reactions take place wherein calcium carbonate precipitate and lanthanum carbonate precipitate are concurrently formed in accordance with ionic reactions 1 and 2 as previously mentioned.

After complete addition of the ammonium carbonate solution, the nitrate solution and the precipitates are mixed in the mixing vat for approximately ten minutes to insure complete precipitation of calcium carbonate and lanthanum carbonate from the nitrate solution and to provide a homogenous mixture of calcium carbonate precipitate and lanthanum carbonate precipitate. The intimately mixed precipitates (i.e. the co-precipitate) of calcium carbonate and lanthanum carbonate facilitate conversion of such calcium and lanthanum sources into the calcium lanthanum sulfide material during subsequent sulfurization in a manner to be described.

The co-precipitate of calcium carbonate and lanthanum carbonate is then filtered from the nitrate solution, cleaned by distilled water, and is then dried in a vacuum oven at approximately 110° C. for twenty-four to seventy-two hours. A highly agglomerated homogenous, intimately mixed mass of calcium carbonate and lanthanum carbonate is provided after drying of the precipitate, as previously described in conjunction with FIG. 1. The calcium carbonate and the lanthanum carbonate are intimately mixed and uniformly distributed throughout the agglomerated mass. The calcium carbonate and lanthanum carbonate agglomerated mass is broken up into a starting powder, as previously shown in FIG. 2B, by conventional techniques such as using a mortar and pestle prior to further processing of such material. The calcium carbonate and lanthanum carbonate starting powders have a microstructure having particles which are substantially uniform and small in size, as previously described.

The starting powder is then sulfurized to convert such starting powder into a solid solution of calcium lanthanum sulfide and γ phase lanthanum sulfide. This is accomplished as follows: The intimately mixed calcium carbonate and lanthanum carbonate starting powder is disposed in an alumina boat and the alumina boat is then placed in an alumina reaction tube furnace as previously described in conjunction with FIG. 1. The interior of the tube is purged of atmospheric gases by directing a continuous flow of helium or another inert gas into the tube. The flow rate for the helium gas is typically 20 SCCM (standard cubic centimeters per minute). The furnace is then raised to a predetermined, elevated temperature of at least 900° C. Here a preferred elevated temperature of 1000° C. is used. At the preferred elevated temperature of 1000° C. and with the continuous flow of helium gas, a predetermined continuous flow rate of hydrogen sulfide gas (H₂ S) is directed over the calcium carbonate and lanthanum carbonate starting powder. Here the flow rate for the hydrogen sulfide gas for 394 grams of calcium carbonate and lanthanum carbonate starting powder is 680 SCCM. A continuous flow of hydrogen sulfide is provided for here approximately 20 hours at 1000° C. In response to such flow of hydrogen sulfide at the elevated temperature, a reaction takes place by diffusion of sulfur into the carbonate powder in accordance with unbalanced reaction 4 to provide 284 grams of calcium lanthanum sulfide and the binary sulfide, lanthanum sulfide La₂ S₃ :

    2La.sub.2 (CO.sub.3).sub.3 +CaCO.sub.3 +7H.sub.2 S→CaLa.sub.2 S.sub.4 +La.sub.2 S.sub.3 +7H.sub.2 O+7CO.sub.2           (Reaction 4)

Here an excess or predetermined amount of lanthanum nitrate in relation to the amount of calcium nitrate is provided in the nitrate solution, with more than 2.0 moles of lanthanum being provided for each mole of calcium. With this composition, and after subsequent sulfurization at a temperature of at least 900° C. as described above, calcium lanthanum sulfide and the binary sulfide, lanthanum sulfide, are believed formed. The phase or structure type of lanthanum sulfide believed formed is gamma (γ) phase lanthanum sulfide. Formation of γ phase lanthanum sulfide is preferable to the binary sulfide calcium sulfide or other phases of lanthanum sulfide such as β lanthanum sulfide because γ phase lanthanum sulfide has a crystallographic structure substantially the sam as that of calcium lanthanum sulfide whereas the binary sulfides β lanthanum sulfide and calcium sulfide have crystallographic structures which are substantially different than the crystallographic structure of calcium lanthanum sulfide. Gamma phase lanthanum sulfide is thus believed to form a solid solution with the calcium lanthanum sulfide. Because the calcium lanthanum sulfide and the γ lanthanum sulfide have substantially the same crystallographic structure after densification, an optically transmittant body having a high degree of transmittance is provided, as will be described hereinafter.

It is to be noted that after sulfurization, two types of material are believed present in the product produced from the sulfurization. The first material, being substantially all of the sulfurization product, is believed to be the solid solution of calcium lanthanum sulfide and γ lanthanum sulfide having a slightly yellowish appearance when observed. The second material present in the sulfurization product is believed to be partially sulfurized material, which is deficient in sulfur, or unsulfurized calcium carbonate and lanthanum carbonate. The second material has a whitish appearance and is substantially completely converted to calcium lanthanum sulfide or lanthanum sulfide during a subsequent sintering in a hydrogen sulfide atmosphere.

The solid solution of calcium lanthanum sulfide and γ lanthanum sulfide is also a well-agglomerated mass which is broken up into smaller sized particles to increase the surface area of the material, as previously described, by grinding the material with a mortar and pestle with a predetermined amount of methanol having previously been added to the material. A 400 mesh sieve is then used to filter out particles having a dimension greater than 37 microns. The filtered calcium lanthanum sulfide and γ lanthanum sulfide material is then dried out by evaporating the methanol providing a powder of the solid solution of calcium lanthanum sulfide and γ lanthanum sulfide as shown in FIG. 7.

Having formed the calcium lanthanum sulfide and γ lanthanum sulfide solid solution powder, the powder is then processed into the optically transmittant body. The processing for forming the body is substantially the same as previously described including the steps of molding, cold pressing, sintering and hot isostatically pressing.

During sintering, however, the temperature of such furnace is elevated to approximately 1150° C. while maintaining an atmospheric pressure and a continuous helium flow in the furnace. Sintering takes place at the elevated temperature of 1150° C. for approximately two hours by passing a continuous flow of helium having a flow rate of here 50 SCCM and hydrogen sulfide having a flow rate of 15 SCCM, as a reactive gas, across the sample disposed on the boron nitride setter plate. The presence of the hydrogen sulfide gas during sintering aids in preventing decomposition of the calcium lanthanum sulfide and γ lanthanum sulfide material at the elevated temperature by preventing sulfur from leaving the material. The sulfur rich environment also aids in the conversion of any unconverted calcium carbonate or lanthanum carbonate material or any material deficient in sulfur provided from the sulfurization step which might be present in the consolidated material, as mentioned above. After sintering, the calcium lanthanum sulfide and γ lanthanum sulfide material has achieved an actual density in the range of approximately 91 to 95% of its theoretical density.

As shown in FIG. 8A, the microstructure of the surface of the body is comprised of isolated closed pores and small grains of such material.

The material, after sintering, is then processed by a technique commonly referred to as hot isostatic pressing, as previously described. The body is hot isostatically pressed at a temperature of 990° C. and a pressure of 29,000 psi for approximately three hours. At the completion of this process, a body having a density of at least 99.5% of the theoretical density of such material is obtained.

As shown in FIG. 8B, the microstructure of the surface of the body after hot isostatic pressing provides material having substantially no porosity without substantially changing the grain size of the material provided during the sintering step. The fabricated body is then ground and polished to predetermined specifications of thickness and surface quality using conventional techniques.

With the above-described process, several advantages in providing bodies comprising a ternary sulfide in solid solution with a binary sulfide is provided.

Again, as shown in FIG. 2B, the concurrently precipitated calcium carbonate and lanthanum carbonate particles are intimately mixed, providing a homogenous starting powder and are of relatively small and substantially uniform particle size. Sulfurization of such starting powder to provide the solid solution of calcium lanthanum sulfide and γ lanthanum sulfide is significantly easier and provides substantially complete conversion of the calcium carbonate and lanthanum carbonate to the calcium lanthanum sulfide and γ lanthanum sulfide, as previously described.

By providing an excess amount of lanthanum, all of the calcium present combines with lanthanum to provide additional calcium lanthanum sulfide, and there is substantially no calcium remaining to form the undesirable calcium sulfide. Thus, adding an excess amount of lanthanum prevents formation of calcium sulfide in the calcium lanthanum sulfide material. Further, any excess lanthanum is so processed to provide γ phase lanthanum sulfide which has substantially the same crystal structures as, and is in solid solution with, calcium lanthanum sulfide.

As shown in FIG. 9, an x-ray diffraction pattern of a sample of calcium lanthanum sulfide and γ phase lanthanum sulfide material made from the co-precipitation of calcium carbonate and excess lanthanum carbonate as described above and processed by the above-described sulfurization step for twenty hours in a helium/hydrogen sulfide atmosphere at an elevated temperature of 1000° C. does not exhibit the peaks 40, 42 (FIG. 5A) generally associated with the calcium sulfide as depicted in FIG. 5A.

As also noted, the addition of excess lanthanum processed in accordance with the techniques described above provides lanthanum sulfide which has a similar crystallographic structure as calcium lanthanum sulfide. An X-ray diffraction analysis of the material thus does not exhibit any peaks which are uncharacteristic of calcium lanthanum sulfide. That is because the peaks of the phase lanthanum sulfide, believed present, are masked by the peaks provided by the calcium lanthanum sulfide because of the substantially identical crystal structure. Thus, the calcium lanthanum sulfide and lanthanum sulfide fabricated by providing an excess amount of lanthanum in relation to calcium and sulfurized at a temperature in excess of 900° C. have the same crystallographic structure. Thus, the solid solution of calcium lanthanum sulfide and lanthanum sulfide is a substantially phase-pure composition, being substantially depleted of β phase lanthanum sulfide and calcium sulfide.

Referring now to FIG. 10, a graph of in-line infrared percent transmittance for the solid solution of calcium lanthanum sulfide and γ lanthanum sulfide material fabricated in accordance with the alternate embodiment of the present invention is shown for a sample (a) having a thickness of 15 mil (0.015 inch) (curve a) and a sample (b) having a thickness of 48 mil (0.048 inch) (curve b). It is to be noted that the optical transmittance (at 50% transmittance) for both samples is at least 16 microns.

                  TABLE 2                                                          ______________________________________                                                  % Transmittance                                                                             % Transmittance (T.sub.2)                                Wavelength                                                                              (T.sub.1) Sample A                                                                          Sample B                                                 (Microns)                                                                               t.sub.1 = 0.015 inches                                                                      t.sub.2 = 0.048 inches                                                                        (cm.sup.-1)                               ______________________________________                                          4       57           57             <0.1                                       6       60           60             <0.1                                       8       62           61             0.194                                     10       65           63             0.373                                     12       67           63             0.735                                     14       67           61             1.120                                     16       65           51             2.895                                     18       50           20             10.934                                    ______________________________________                                    

From the values of percent transmittance from each curve a,b, a characteristic of the material which indicates the degree of absorption of such material of electromagnetic radiation in The range of 4 to 18 microns is obtained from the equation α=[-ln (T_(b) /T_(a))]/(t_(b) t_(a)) where α is a quantity referred to as the "coefficient of absorption," T_(a), T_(b) are the percent transmittance of samples a, b, respectively, and t_(a), t_(b) are thicknesses of samples a, b, respectively. As shown in Table 2, for the material fabricated in accordance with the present invention, α is in the range of <0.1 cm⁻¹ to 2.89 cm⁻¹ for electromagnetic radiation having a wavelength in the range of 4 microns to 16 microns. Thus, the relatively low coefficient of absorption of such material indicates that the percent transmittance of such material for thicker samples will be relatively high.

Having described preferred embodiments of the invention, it will now be apparent to one of skill in the art that other embodiments incorporating its concept may be used. For example, other ratios of calcium nitrate and lanthanum nitrate may be used as well as other sources of calcium and lanthanum cations. Further, other cations such as strontium and neodymium may also be used. It is felt, therefore, that this invention should not be limited to the disclosed embodiment, but rather should be limited only by the spirit and scope of the appended claims. 

What is claimed is:
 1. A method of forming an optically transmissive body comprising a binary sulfide and a ternary sulfide said ternary sulfide having two cation types, a first one selected from the group consisting of metal cations, a second one selected fro the group consisting of the lanthanum series cations comprising the steps of:reacting the two cation types with a material which when reacted provides a source of sulfide anions to convert all of said first cation type and a first portion of said second cation type into the ternary sulfide, and reacting a second remaining portion of said second cation type into the binary sulfide, said binary sulfide forming a solid solution with said ternary sulfide with said metal cations and lanthanum series cations selected from those which will form a binary sulfide ternary sulfide solution; and forming the binary sulfide and ternary sulfide into the optically transmissive body.
 2. A method for forming an optically transmissive body comprising a ternary sulfide in solid solution with a binary sulfide comprising the steps of:forming a precursor powder having a pair of cation types, a first one selected from the group consisting of calcium and strontium and a second one selected from the group consisting of lanthanum and neodymium in a predetermined nonstoichiometric composition of said ternary sulfide to provide an excess amount of said second cation type; reacting the powder with a material which when reacted provides a source of sulfide anions to convert a first portion of said powder into the ternary sulfide, and a remaining portion of said powder into the binary sulfide having the second type cation, said binary sulfide forming a solid solution with said ternary sulfide; and processing the binary sulfide and ternary sulfide into the optically transmissive body.
 3. A method for providing an optically transmissive body comprising calcium lanthanum sulfide in solid solution with lanthanum sulfide comprising the steps of:forming a starting powder including calcium cations and lanthanum cations in a ratio of greater than 2 moles of lanthanum cations to 1 mole of calcium cations; reacting the starting powder with a material which when reacted provides a source of a sulfide anion to convert a first portion of said powder into the calium lanthanum sulfide, and a remaining portion of such starting powder into lanthanum sulfide, said lanthanum sulfide forming a solid solution with said calcium lanthanum sulfide; and processing the solid solution of lanthanum sulfide and calcium lanthanum sulfide into the optically transmissive body.
 4. A method of forming an optically transmissive body comprising a solid solution of a calcium lanthanum sulfide and lanthanum sulfide comprising the steps of:forming a starting powder including calcium and lanthanum cations in the ratio of greater than 2.0 moles of lanthanum to 1.0 moles of calcium; reacting at an elevated temperature of at least 900° C. the starting powder with a material which when reacted provides a source of sulfide anions to convert a first portion of the lanthanum cations and all the calcium cations into calcium lanthanum sulfide, and the remaining portion of lanthanum cations into the lanthanum sulfide forming a solid solution with said calcium lanthanum sulfide; and processing the solid solution of calcium lanthanum sulfide and lanthanum sulfide into the optically transmissive body.
 5. The method as recited in claim 4 wherein the step of forming the body further comprises the steps of:consolidating the solid solution into the body, providing said solution with a predetermined density; sintering the solid solution in an environment of a material which when reacted provides a source of sulfide anions, at an elevated temperature in the range of 900° C. to 1200° C. providing the body with a density in the range of 91 to 95%; and compressing the body at an elevated pressure of at least 20,000 psi and at an elevated temperature in the range of 900° C. to 1100° C. providing said solid solution with a density of at least 99%.
 6. The method as recited in claim 4 wherein the starting powder reacts with the sulfide anions at an elevated temperature of 1000° C.
 7. The method as recited in claim 3 wherein the reacting step further comprises:directing at an elevated temperature in the range of 900° C. to 1100° C. a flow of hydrogen sulfide gas over the starting powder to convert said powder into the calcium lanthanum sulfide and lanthanum sulfide.
 8. The method as recited in claim 7 wherein the elevated temperature is about 1000° C.
 9. The method as recited in claim 8 wherein the processing step further comprises the steps of:consolidating the solid solution of lanthanum sulfide and calcium lanthanum sulfide into the body having a first density; sintering said consolidated body at an elevated temperature in the presence of hydrogen sulfide until said body has a density between 91% and 95% of theoretical density; and compressing said solution at an elevated pressure and at an elevated temperature to provide said body having an actual density of at least 99.5% of theoretical density.
 10. A method as recited in claim 9 wherein during said compressing step, the body is compressed to provide said optically transmissive body, with a sample of said compressed body, having a thickness of 0.048 inches, has an optical transmissivity of at least 50% to energy having a wavelength in the range of 4.0 microns to at least 16.0 microns.
 11. The method as recited in claim 9 wherein during said compressing step, the body is compressed to provide said optically transmissive body, with a first sample of said body having a first thickness of 0.048 inches has an optical transmissivity of at least 50% and a second sample of said body having a second thickness of about 0.015 inches has an optical transmissivity of at least 50%, eand transmissivity being over the range of at least 0.4 microns to 16.0 microns.
 12. The method as recited in claim 11 wherein said body has a coefficient of absorption α of less than 3.0 over said optical wavelength range where α is given by α=[1n(T_(b) /T_(a))]/(t_(b) -t_(a)) where T_(a), T_(b) are the percent transmissivity of the first and second samples and t_(a), t_(b) are the first and second thickness.
 13. The method as recited in claim 12 wherein α is less than 1.0 over the optical range of 4.0 microns to 12.0 microns.
 14. The method as recited in claim 13 wherein a sample of said body has an optical transmissivity of at least 60% over the wavelength range of 8-12 microns for a thickness of said sample in the range of 0.015 to 0.048 inches.
 15. The method as recited in claim 6 wherein during said compressing step, the body is compressed to provide said optically transmissive body, with a sample of said body, having a thickness of 0.048 inches, has an optical transmissivity of at least 50% to energy having a wavelength in the range of 4.0 microns to 16.0 microns.
 16. The method as recited in claim 6 wherein during said compressing step, the body is compressed to provide said optically transmissive body, with a first sample of said body, having a first thickness of 0.048 inches, has an optical transmissivity of at least 50%, and a second sample of said body, having a second thickness of about 0.015 inches, has an optical transmissivity of at least 50%, each transmissivity being over the range of 4.0 microns to 16.0 microns.
 17. The method as recited in claim 16 wherein said body has a coefficient of absorption α of less than 3.0 over said optical wavelength range where α is given by α=[1n(T_(b) /T_(a))]/(t_(b) -t_(a)) where T_(a), T_(b) are the percent transmissivity of the first and second samples and t_(a), t_(b) are the first and second thickness.
 18. The method as recited in claim 17 wherein α is less than 1.0 over the optical range of 4.0 microns to 12.0 microns.
 19. The method as recited in claim 18 wherein a sample of said body has an optical transmissivity of at least 60% over the wavelength range of 8-12 microns, for a thickness of said sample the range of 0.015 to 0.048 inches. 